Is Nuvialab Limited on an FDA import alert?

No listing for Nuvialab Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Cyprus page.

Has FDA refused shipments from Nuvialab Limited?

Yes. FDA refused 5 shipment lines from Nuvialab Limited on June 2, 2020. The most recent, on June 2, 2020, was l-arginine (protein), charged as UNAPPROVED (unapproved new drug).

Why did FDA refuse Nuvialab Limited's shipments?

The most frequent charge is UNAPPROVED (unapproved new drug, 5 lines).

What is Nuvialab Limited's FEI number?

Nuvialab Limited's FDA Establishment Identifier (FEI) is 3016619331.

Nuvialab Limited

FDA import alert and refusal historyLimassol, CyprusFEI 3016619331

Recorded by FDA as NUVIALAB LIMITED

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As of October 26, 2026, Nuvialab Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines on June 2, 2020, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Jun 2, 2020L-arginine (protein) · UNAPPROVED
Last warning letter: None found
Last inspection: None on record

Every FDA record for Nuvialab Limited

5 records, newest first. Each line links to the FDA page it came from.

2020

Jun 2, 2020Import refusal
Refused, L-arginine (protein)UNAPPROVEDEntry SCS-9460474-2
Source
Jun 2, 2020Import refusal
Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-9470464-1
Source
Jun 2, 2020Import refusal
Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-0120598-0
Source
Jun 2, 2020Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry SCS-9465611-4
Source
Jun 2, 2020Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry SCS-0191396-3
Source

Refusal charges, in plain English

UNAPPROVED5 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Nuvialab Limited

Is Nuvialab Limited on an FDA import alert?: No listing for Nuvialab Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Cyprus page.
Has FDA refused shipments from Nuvialab Limited?: Yes. FDA refused 5 shipment lines from Nuvialab Limited on June 2, 2020. The most recent, on June 2, 2020, was l-arginine (protein), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Nuvialab Limited's shipments?: The most frequent charge is UNAPPROVED (unapproved new drug, 5 lines).
What is Nuvialab Limited's FEI number?: Nuvialab Limited's FDA Establishment Identifier (FEI) is 3016619331.

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.